Evidence map›Paper›PMID 40610616›Full record

ArticleCommunications medicine2025

Cognitive characteristics and ischemic prognosis of quantitative white matter hyperintensities in adult moyamoya disease.

Ziqi Liu, Xiaokuan Hao, Qi Duan, Chaoran Shen, Haojin Lyu, Junze Zhang, Jing Gu, Shihao He, Yanru Wang, Xilong Wang and 6 more

Abstract read
In one paragraph

Article in Communications medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

16 authors.

Ziqi Liu *Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Xiaokuan Hao *Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Qi DuanDepartment of Radiology, Chinese PLA General Hospital, Beijing, China.
Chaoran ShenState Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China.
Haojin LyuDepartment of Radiology, Chinese PLA General Hospital, Beijing, China.
Junze ZhangDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Jing GuDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Shihao HeDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.ORCID http://orcid.org/0000-0002-2522-8656
Yanru WangDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Xilong WangDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Zhenyu ZhouDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Ning MaDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Ran DuanDepartment of Neurosurgery, Peking University International Hospital, Beijing, China.
Xinlin ZhouState Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China.
Xin LouDepartment of Radiology, Chinese PLA General Hospital, Beijing, China. louxin@301hospital.com.cn.
Rong WangDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China. ronger090614@ccmu.edu.cn.ORCID http://orcid.org/0000-0002-0669-9321

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82171887
6 · The paper itself

Abstract

backgroundWhite matter hyperintensities (WMHs) are associated with long-term stroke and cognitive decline in the elderly population but differ from the young and middle-aged populations, especially for those with moyamoya disease (MMD). The aim of this study was to modify the Fazekas grade and quantitatively analyze the effects of WMHs on multiple cognitive domains and 2-year clinical ischemic events in adult MMD patients.

methodsAdult MMD patients and healthy controls were recruited for a comprehensive cognitive assessment. Among 151 adult MMD patients, the average age was 41.78 ± 10.59 years and the male-to-female ratio was 0.94. Adjusted quantitative whole-brain, periventricular (PVWMHs), and deep WMHs (DWMHs) were included in the proportional hazards model to explore their relationships with 2-year ischemic events. Linear regression analysis was used to evaluate the correlation between the WMH burden in different brain regions and various cognitive domains.

resultsMMD patients present decreases in intelligence (P = 0.000), spatial working memory (P = 0.011), verbal working memory 1 (P = 0.000) and 2 (P = 0.000), mental rotation (P = 0.008), and executive inhibition (P = 0.011). Quantitative whole-brain log

conclusionsPVWMHs have greater potential effects on verbal working memory, attention, and simple subtraction in adult MMD patients when compared with DWMHs. An increase in PVWMHs could be an indicator of future ischemic events in adults with MMD. CLINICAL REGISTRATION: Clinical registration no. ChiCTR2200058251 URL: https://www.chictr.org.cn/ .

Identifiers

PMID40610616
PMCPMC12229540

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